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Loss of ferritin‐positive microglia relates to increased iron, RNA oxidation, and dystrophic microglia in the brains of aged male marmosets

Bibliographic Data

ID19386609
AuthorsJuan de Dios Rodríguez‐Callejas (Department of Pharmacology Center of Research in Advance Studies Mexico City Mexico), Juan D Rodríguez-Callejas (0000-0002-7365-1408), Daniel Cuervo‐Zanatta (Department of Pharmacology Center of Research in Advance Studies Mexico City Mexico), Daniel Cuervo-Zanatta (0000-0002-3104-1679), Abraham Rosas‐Arellano (0000-0003-1422-9538, Department of Pharmacology Center of Research in Advance Studies Mexico City Mexico), Caroline Fonta (0000-0001-6326-4044, Brain and Cognition Research Centre (CERCO) CNRS/University of Toulouse Toulouse France), Eberhard Fuchs (German Primate Center Leibniz Institute for Primate Research Göttingen Germany), Claudia Perez‐Cruz (0000-0002-5983-307X, Department of Pharmacology Center of Research in Advance Studies Mexico City Mexico, corresponding author)
Year2019
Volume81
Issue2
Pagese22956-e22956
Publication date2019-02-01
Open AccessYes
TypeARTICLE
VenueAmerican Journal of Primatology (JOURNAL)
Journal identifiersISSN: 0275-2565 • E-ISSN: 1098-2345
PublisherWiley (PUBLISHER • GB)
DOI10.1002/ajp.22956
PMID30779205
OpenAlexW2916936332
LanguageEN
Citations received1
References cited90

Microglia are cells that protect brain tissue from invading agents and toxic substances, first by releasing pro-inflammatory cytokines, and thereafter by clearing tissue by phagocytosis. Microglia express ferritin, a protein with ferroxidase activity capable of storing iron, a metal that accumulates in brain during aging. Increasing evidence suggests that ferritin plays an important role in inflammation. However, it is not known if ferritin/iron content can be related to the activation state of microglia. To this end, we aimed to delineate the role of ferritin in microglia activation in a non-human primate model. We analyzed brains of male marmosets and observed an increased density of ferritin+ microglia with an activated phenotype in hippocampus and cortex of old marmosets (mean age 11.25 ± 0.70 years) compared to younger subjects. This was accompanied by an increased number of dystrophic microglia in old marmosets. However, in aged subjects (mean age 16.83 ± 2.59 years) the number of ferritin+ microglia was decreased compared to old ones. Meanwhile, the content of iron in brain tissue and cells with oxidized RNA increased during aging in all hippocampal and cortical regions analyzed. Abundant amoeboid microglia were commonly observed surrounding neurons with oxidized RNA. Notably, amoeboid microglia were arginase1+ and IL-10+, indicative of a M2 phenotype. Some of those M2 cells also presented RNA oxidation and a dystrophic phenotype. Therefore, our data suggest that ferritin confers protection to microglia in adult and old marmosets, while in aged subjects the decline in ferritin and the increased amount of iron in brain tissue may be related to the increased number of cells with oxidized RNA, perhaps precluding the onset of neurodegeneration

Biology · Ferritin · Hippocampal formation · Inflammation · Microglia · Phagocytosis · Alzheimer's disease research and treatments · Barrier Structure and Function Studies · Chemistry · Neuroinflammation and Neurodegeneration Mechanisms · Biochemistry · Cell Biology · Endocrinology · Immunology

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Citations per year0.2
Citation span2021 - 2021 (1)
Highly citedNo

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